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Loss of function of C9orf72 causes motor deficits in a zebrafish model of amyotrophic lateral sclerosis

Annals of neurology, 2013-08, Vol.74 (2), p.180-187

2013

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Transient Receptor Potential Vanilloid 1 Is Required for Intrinsic Osmoreception in Organum Vasculosum Lamina Terminalis Neurons and for Normal Thirst Responses to Systemic Hyperosmolality

The Journal of neuroscience, 2006-08, Vol.26 (35), p.9069-9075

2006

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Understanding the Role of the SMN Complex Component GEMIN5 and Its Functional Relationship with Demethylase KDM6B in the Flunarizine-Mediated Neuroprotection of Motor Neuron Disease Spinal Muscular Atrophy

International journal of molecular sciences, 2024-09, Vol.25 (18), p.10039

2024

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The most prevalent genetic cause of ALS-FTD, C9orf72 synergizes the toxicity of ATXN2 intermediate polyglutamine repeats through the autophagy pathway

Autophagy, 2016-08, Vol.12 (8), p.1406-1408

2016

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ΔN-TRPV1: A Molecular Co-detector of Body Temperature and Osmotic Stress

Cell reports (Cambridge), 2015-10, Vol.13 (1), p.23-30

2015

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Methylene blue protects against TDP-43 and FUS neuronal toxicity in C. elegans and D. rerio

PloS one, 2012-07, Vol.7 (7), p.e42117

2012

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TDP-43 Regulation of AChE Expression Can Mediate ALS-Like Phenotype in Zebrafish

Cells (Basel, Switzerland), 2021-01, Vol.10 (2), p.221

2021

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Trpv4 Mediates Hypotonic Inhibition of Central Osmosensory Neurons via Taurine Gliotransmission

Cell reports (Cambridge), 2018-05, Vol.23 (8), p.2245-2253

2018

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Microglia Mitigate Neuronal Activation in a Zebrafish Model of Dravet Syndrome

Cells (Basel, Switzerland), 2024-04, Vol.13 (8), p.684

2024

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Neuromuscular Junction Impairment in Amyotrophic Lateral Sclerosis: Reassessing the Role of Acetylcholinesterase

Frontiers in molecular neuroscience, 2016-12, Vol.9, p.160-160

2016

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Neuroleptics as therapeutic compounds stabilizing neuromuscular transmission in amyotrophic lateral sclerosis

JCI insight, 2017-11, Vol.2 (22)

2017

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Osmotic and thermal control of magnocellular neurosecretory neurons - role of an N-terminal variant of trpv1

The European journal of neuroscience, 2010-12, Vol.32 (12), p.2022-2030

2010

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TANGO2-related rhabdomyolysis symptoms are associated with abnormal autophagy functioning

Autophagy reports, 2024-12, Vol.3 (1)

2024

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Depdc5 knockdown causes mTOR‐dependent motor hyperactivity in zebrafish

Annals of clinical and translational neurology, 2018-05, Vol.5 (5), p.510-523

2018

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Overexpression of the serine elastase inhibitor elafin protects transgenic mice from hypoxic pulmonary hypertension

Circulation (New York, N.Y.), 2002-01, Vol.105 (4), p.516-521

2002

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Association of Rare Genetic Variants in Opioid Receptors with Tourette Syndrome

Tremor and other hyperkinetic movements (New York, N.Y.), 2019-11, Vol.9, p.1-9

2019

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Novel genome-editing-based approaches to treat motor neuron diseases: Promises and challenges

Molecular therapy, 2022-01, Vol.30 (1), p.47-53

2022

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Defining the genetic connection linking amyotrophic lateral sclerosis (ALS) with frontotemporal dementia (FTD)

Trends in genetics, 2015-05, Vol.31 (5), p.263-273

2015

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Hypertonicity sensing in organum vasculosum lamina terminalis neurons: a mechanical process involving TRPV1 but not TRPV4

The Journal of neuroscience, 2011-10, Vol.31 (41), p.14669-14676

2011

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Neurophysiological characterization of mammalian osmosensitive neurones

Experimental physiology, 2007-05, Vol.92 (3), p.499-505

2007

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Loss of C9ORF72 impairs autophagy and synergizes with polyQ Ataxin-2 to induce motor neuron dysfunction and cell death

The EMBO journal, 2016-06, Vol.35 (12), p.1276-1297

2016

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Sqstm1 knock-down causes a locomotor phenotype ameliorated by rapamycin in a zebrafish model of ALS/FTLD

Human molecular genetics, 2015-03, Vol.24 (6), p.1682-1690

2015

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Poly-GP accumulation due to C9orf72 loss of function induces motor neuron apoptosis through autophagy and mitophagy defects

Autophagy, 2024-10, Vol.20 (10), p.2164-2185

2024

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Behavioral And Physiological Analysis In A Zebrafish Model Of Epilepsy

Journal of visualized experiments, 2021-10 (176)

2021

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Loss of function of C9orf72 causes motor deficits in a zebrafish model of amyotrophic lateral sclerosis

Transient Receptor Potential Vanilloid 1 Is Required for Intrinsic Osmoreception in Organum Vasculosum Lamina Terminalis Neurons and for Normal Thirst Responses to Systemic Hyperosmolality

Understanding the Role of the SMN Complex Component GEMIN5 and Its Functional Relationship with Demethylase KDM6B in the Flunarizine-Mediated Neuroprotection of Motor Neuron Disease Spinal Muscular Atrophy

The most prevalent genetic cause of ALS-FTD, C9orf72 synergizes the toxicity of ATXN2 intermediate polyglutamine repeats through the autophagy pathway

ΔN-TRPV1: A Molecular Co-detector of Body Temperature and Osmotic Stress

Methylene blue protects against TDP-43 and FUS neuronal toxicity in C. elegans and D. rerio

TDP-43 Regulation of AChE Expression Can Mediate ALS-Like Phenotype in Zebrafish

Trpv4 Mediates Hypotonic Inhibition of Central Osmosensory Neurons via Taurine Gliotransmission

Microglia Mitigate Neuronal Activation in a Zebrafish Model of Dravet Syndrome

Neuromuscular Junction Impairment in Amyotrophic Lateral Sclerosis: Reassessing the Role of Acetylcholinesterase

Neuroleptics as therapeutic compounds stabilizing neuromuscular transmission in amyotrophic lateral sclerosis

Osmotic and thermal control of magnocellular neurosecretory neurons - role of an N-terminal variant of trpv1

TANGO2-related rhabdomyolysis symptoms are associated with abnormal autophagy functioning

Depdc5 knockdown causes mTOR‐dependent motor hyperactivity in zebrafish

Overexpression of the serine elastase inhibitor elafin protects transgenic mice from hypoxic pulmonary hypertension

Association of Rare Genetic Variants in Opioid Receptors with Tourette Syndrome

Novel genome-editing-based approaches to treat motor neuron diseases: Promises and challenges

Defining the genetic connection linking amyotrophic lateral sclerosis (ALS) with frontotemporal dementia (FTD)

Hypertonicity sensing in organum vasculosum lamina terminalis neurons: a mechanical process involving TRPV1 but not TRPV4

Neurophysiological characterization of mammalian osmosensitive neurones

Loss of C9ORF72 impairs autophagy and synergizes with polyQ Ataxin-2 to induce motor neuron dysfunction and cell death

Sqstm1 knock-down causes a locomotor phenotype ameliorated by rapamycin in a zebrafish model of ALS/FTLD

Poly-GP accumulation due to C9orf72 loss of function induces motor neuron apoptosis through autophagy and mitophagy defects

Behavioral And Physiological Analysis In A Zebrafish Model Of Epilepsy

Chloride deregulation and GABA depolarization in MTOR related malformations of cortical development

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